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S-phenyl naphthalene-2-carbothioate

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Identification
Molecular formula
C17H12OS
CAS number
81981-76-6
IUPAC name
S-phenyl naphthalene-2-carbothioate
State
State
This compound is in a solid state at room temperature, and typically forms crystalline structures.
Melting point (Celsius)
78.00
Melting point (Kelvin)
351.00
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.00
General information
Molecular weight
292.39g/mol
Molar mass
292.3900g/mol
Density
1.2000g/cm3
Appearence
This compound is typically a crystalline solid with a pale-yellow appearance. The crystals are often shiny or lustrous, and the substance is generally powdery when in a fine state.
Comment on solubility

Solubility of S-phenyl naphthalene-2-carbothioate

S-phenyl naphthalene-2-carbothioate is a fascinating compound with unique solubility characteristics. Understanding its solubility is essential for various applications in chemical processes. Here are some key points regarding its solubility:

  • Solvent Compatibility: S-phenyl naphthalene-2-carbothioate is typically soluble in organic solvents such as ethanol, acetone, and chloroform. This solubility in organic mediums makes it applicable in non-aqueous reactions.
  • Aqueous Solubility: The compound exhibits poor solubility in water, which is common among many organic thiocarbonates due to their hydrophobic nature.
  • Influencing Factors: The solubility of this compound can be influenced by temperature and the presence of other solutes. Increased temperatures generally improve solubility in organic solvents.
  • Miscibility: It is important to note that while S-phenyl naphthalene-2-carbothioate is suitable for many organic reactions, complete miscibility with certain solvents may still pose limitations in specific formulations or applications.

In summary, understanding the solubility of S-phenyl naphthalene-2-carbothioate helps in designing experiments and formulating processes where this compound is utilized. Its distinctive solubility pattern highlights the need for careful solvent selection in practical applications.

Interesting facts

Interesting Facts about S-phenyl naphthalene-2-carbothioate

S-phenyl naphthalene-2-carbothioate is a fascinating compound that offers a variety of intriguing possibilities in the realm of chemistry and materials science. Here are some interesting insights about this compound:

  • Unique Structure: This compound features a naphthalene ring, which is known for its stability and aromatic properties, combined with a carbothioate functional group. This *unique hybrid structure* enhances its chemical reactivity.
  • Synthesis: The synthesis of S-phenyl naphthalene-2-carbothioate typically involves a reaction between naphthalene derivatives and thiol compounds. This pathway illustrates the versatility and importance of organosulfur compounds in synthetic organic chemistry.
  • Applications: Compounds like S-phenyl naphthalene-2-carbothioate have potential applications in various fields such as:
    • Material Science: As precursors in the synthesis of polymers and dyes.
    • Pharmaceutical Industry: In the development of drugs due to its biological activity.
    • Organic Electronics: Potential use in organic semiconductors.
  • Biological Activity: Certain carbothioate derivatives have shown *antimicrobial and antioxidant properties,* thus making them interesting subjects for further investigation in medicinal chemistry.
  • Research Potential: Ongoing studies are examining how slight modifications of its structure can enhance its properties. This makes it a platform for *research on structure-activity relationships* in chemical librettos.

In conclusion, S-phenyl naphthalene-2-carbothioate is not just another compound; it embodies the *intersection of chemistry, industry, and innovation,* making it a significant topic for students and researchers alike.

Synonyms
S-Phenyl 2-naphthalenethiocarboxylate
28118-49-2
2-NAPHTHOIC ACID, S-PHENYL ESTER
2-Naphthalenecarboxylic acid, thio-, S-phenyl ester
DTXSID80182393
RefChem:264222
DTXCID90104884
S-phenyl naphthalene-2-carbothioate